Trabecular Metal Reverse PlusRecalls & reported problems across all models
Zimmer, Inc. · 10 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 30
- Deaths reported
- 0
- Injuries reported
- 30
- Recalls
- 0
We found 10 models of Trabecular Metal Reverse Plus by Zimmer, Inc. in the FDA's device registry (GUDID). Together they are named in 30 adverse event reports in the FDA's MAUDE database, received between Jun 26, 2020 and Feb 23, 2026 — classified as 30 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (19 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Trabecular Metal Reverse Plus problems
Device problems
- Detachment of Device or Device Component19
- Device Dislodged or Dislocated5
- Adverse Event Without Identified Device or Use Problem3
- Loosening of Implant Not Related to Bone-Ingrowth2
- Fracture1
- Noise, Audible1
Patient problems
- Failure of Implant14
- Joint Dislocation9
- No Clinical Signs, Symptoms or Conditions4
- Pain3
- Discomfort2
- Pneumonia2
- Pulmonary Embolism2
- Bone Fracture(s)1
Trabecular Metal Reverse Plus models
10 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Trabecular Metal Reverse Plus™ 00-4362-015-00PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED7 reports
- Trabecular Metal Reverse Plus™ 00-4360-036-00PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED7 reports
- Trabecular Metal Reverse Plus™ 00-4362-020-00PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED6 reports
- Trabecular Metal Reverse Plus™ 00-4360-040-00PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED3 reports
- Trabecular Metal Reverse Plus™ 00-4362-025-00PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- Trabecular Metal Reverse Plus™ 00-4363-036-00PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- Trabecular Metal Reverse Plus™ 00-4363-040-00PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 report
- Trabecular Metal Reverse Plus™ 00-4363-040-25PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED1 report
- Trabecular Metal Reverse Plus™ 00-4365-040-00shoulder prosthesis, reverse configuration1 report
- Trabecular Metal Reverse Plus™ 00-4365-040-25shoulder prosthesis, reverse configuration1 report
Recent Trabecular Metal Reverse Plus adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryFeb 23, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT A PATIENT HAD AN INITIAL LEFT REVERSE TOTAL SHOULDER ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO COMPONENT DISSOCIATION APPROXIMATELY 1 MONTH POST IMPLANTATION. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24414756 ↗InjuryFeb 23, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT A PATIENT HAD AN INITIAL LEFT REVERSE TOTAL SHOULDER ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO COMPONENT DISSOCIATION APPROXIMATELY 1 MONTH POST IMPLANTATION. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24414728 ↗InjuryJan 8, 2026Detachment of Device or Device Component
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Joint Dislocation
MAUDE report 24003838 ↗InjuryAug 27, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT INITIAL OPERATION WAS PERFORMED AND AN X-RAY WAS TAKEN IMMEDIATELY AFTER THE SURGERY REVEALED THAT THE GLENOSPHERE HEAD HAD BECOME DETACHED. THEREFORE, A REOPERATION WAS PERFORMED ON THE SAME DAY TO REPLACE THE GLENOSPHERE HEAD, AND THE SURGERY WAS COMPLETED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Joint Dislocation
MAUDE report 22903531 ↗InjuryMay 12, 2025Fracture; Detachment of Device or Device Component; Fracture; Detachment of Device or Device Component
IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION PROCEDURE APPROXIMATELY 3 MONTHS POST IMPLANTATION AFTER COMPLAINING OF DISCOMFORT. PRIOR TO THE REVISION, AN X RAY REVEALED WHAT APPEARED TO BE A FRACTURED TAPER THAT HAD DISENGAGED FROM THE GLENOSPHERE. A NEW GLENOSPHERE, BEARING, AND BASEPLATE WERE IMPLANTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Discomfort; Failure of Implant
MAUDE report 22001708 ↗InjuryMay 12, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION PROCEDURE APPROXIMATELY 3 MONTHS POST IMPLANTATION AFTER COMPLAINING OF DISCOMFORT. PRIOR TO THE REVISION, AN X RAY REVEALED WHAT APPEARED TO BE A FRACTURED TAPER THAT HAD DISENGAGED FROM THE GLENOSPHERE. A NEW GLENOSPHERE, BEARING, AND BASEPLATE WERE IMPLANTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Discomfort; Failure of Implant
MAUDE report 22001700 ↗InjuryMar 5, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT SHOULDER ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT RETURNED TO CLINIC FOR EVALUATION DUE TO PAIN. IMAGING CONFIRMED A STRESS FRACTURE LATERAL TO THE GLENOID. PATIENT WORE A SLING FOR FOUR WEEKS TO IMMOBILIZE THE JOINT AND ALSO RECEIVED ADDITIONAL PHYSICAL THERAPY. THE EVENT WAS REPORTED TO BE RESOLVED. APPROXIMATELY ONE-YEAR POST-IMPLANTATION, THE PATIENT WAS NOTED TO HAVE SLIGHT PAIN AND SLIGHT DIFFICULTY WITH ACTIVITIES. NO FURTHER INTERVENTION HAS BEEN REPORTED TO DATE. DUE DILIGENCE IS PROGRESS. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.
Patient problems: Bone Fracture(s); Pain
MAUDE report 21531871 ↗InjuryFeb 3, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Joint Dislocation
MAUDE report 21300106 ↗InjuryFeb 3, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Joint Dislocation
MAUDE report 21300089 ↗InjuryNov 11, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
NO ADDITIONAL INFORMATION IS AVAILABLE REGARDING THE INCIDENT.
Patient problems: Joint Dislocation
MAUDE report 20652239 ↗InjuryMay 6, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION SHOULDER ARTHROPLASTY APPROXIMATELY ONE (1) YEAR AGO AND IS BEING CONSIDERED FOR ANOTHER REVISION DUE TO DISLOCATION ON AN UNKNOWN DATE. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Joint Dislocation
MAUDE report 19255256 ↗InjuryApr 24, 2024Noise, Audible; Noise, Audible
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Joint Dislocation; Pain
MAUDE report 19172363 ↗InjuryMar 14, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL RIGHT TOTAL SHOULDER ARTHROPLASTY APPROXIMATELY A MONTH AGO. SUBSEQUENTLY, 2 DAYS LATER THE PATIENT DEVELOPED PNEUMONIA AND PULMONARY EMBOLISM. MEDICAL TREATMENT INCLUDED ANTIBIOTICS, ANTICOAGULANTS, AND OXYGEN. THE ISSUE WAS RESOLVED 13 DAYS LATER. ATTEMPTS HAVE BEEN MADE AND THERE IS NO FURTHER INFORMATION AT THIS TIME.
Patient problems: Pneumonia; Pulmonary Embolism
MAUDE report 18902597 ↗InjuryMar 14, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL RIGHT TOTAL SHOULDER ARTHROPLASTY APPROXIMATELY A MONTH AGO. SUBSEQUENTLY, 2 DAYS LATER THE PATIENT DEVELOPED PNEUMONIA AND PULMONARY EMBOLISM. MEDICAL TREATMENT INCLUDED ANTIBIOTICS, ANTICOAGULANTS, AND OXYGEN. THE ISSUE WAS RESOLVED 13 DAYS LATER. ATTEMPTS HAVE BEEN MADE AND THERE IS NO FURTHER INFORMATION AT THIS TIME.
Patient problems: Pneumonia; Pulmonary Embolism
MAUDE report 18902590 ↗InjuryDec 19, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant
MAUDE report 18359445 ↗
Other Zimmer, Inc. products
- PERSONA364 models · 2,000 reports · 3 recalls
- Persona The Personalized Knee77 models · 1,396 reports
- PERSONA Vivacit-E285 models · 1,152 reports
- NexGen198 models · 842 reports · 4 recalls
- Affixus18 models · 1 reports · 17 recalls
- PERSONA Natural Tibia25 models · 417 reports · 2 recalls
- NexGen Legacy119 models · 319 reports · 3 recalls
- Alliance32 models · 275 reports · 2 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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